All-inorganic cesium lead halide perovskites have emerged as promising semiconductor materials due to their preeminent performance in lighting, display, light detecting, and laser fields. However, the applications of lead halide perovskites are limited by the dissatisfactory stability owing to their fragile ionic crystal characteristics and highly dynamic surface-coordinated states. The diphase structure passivation possessing the same chemical constituents (such as passivating CsPbBr with CsPbBr) has been proven to be an effective way to improve the stabilities and simultaneously maintain the highly efficient luminescence properties. Herein, for the first time, we report a novel anion-cation reaction method to synthesize the lead halide perovskite NCs with diphase CsPbBr@CsPbBr structure. Moreover, we have found that the phase transformation between CsPbBr and CsPbBr is temperature dependent. Thus, we could control the relative composition of the diphase CsPbBr@CsPbBr composite by adjusting the temperature. The optimized CsPbBr@CsPbBr composite NCs achieve highly light emissive performance and stabilities against atmosphere, moisture and heating. Furthermore, we could obtain 135% of the NTSC color gamut through anion exchange. These highly emissive composite NCs with improved stabilities exhibit great potential in future optoelectronic fields.
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http://dx.doi.org/10.1039/c8na00291f | DOI Listing |
Chemistry
December 2024
East China University of Science and Technology, School of Materials Science and Engineering, meilong Road, 200237, shanghai, CHINA.
Perovskite-based photodetectors (PDs) are broadly utilized in optical communication, non-destructive testing, and smart wearable devices due to their ability to convert light into electrical signals. However, toxicity and instability hold back their mass production and commercialization. The lead-free Cs2AgBiBr6 double perovskite film, promised to be an alternative, is fabricated by electrophoretic deposition (EPD), which compromises film quality.
View Article and Find Full Text PDFACS Nano
December 2024
Department of Materials Science and Engineering, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Collective optical properties can emerge from an ordered ensemble of emitters due to interactions between the individual units. Superlattices of halide perovskite nanocrystals exhibit collective light emission, influenced by dipole-dipole interactions between simultaneously excited nanocrystals. This coupling changes both the emission energy and rate compared to the emission of uncoupled nanocrystals.
View Article and Find Full Text PDFACS Nano
December 2024
Nanochemistry, Istituto Italiano di Tecnologia, Via Morego 30, Genova 16163, Italy.
We report the synthesis of ethylammonium lead iodide (EAPbI) colloidal nanocrystals as another member of the lead halide perovskites family. The insertion of an unusually large -cation (274 pm in diameter) in the perovskite structure, hitherto considered unlikely due to the unfavorable Goldschmidt tolerance factor, results in a significantly larger lattice parameter compared to the Cs-, methylammonium- and formamidinium-based lead halide perovskite homologues. As a consequence, EAPbI nanocrystals are highly unstable, evolving to a nonperovskite δ-EAPbI polymorph within 1 day.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Univ Rennes, ENSCR, CNRS, ISCR-UMR6226, Université de Rennes, Rennes 35042, France.
Metal halide perovskites, including some of their related perovskitoid structures, form a semiconductor class of their own, which is arousing ever-growing interest from the scientific community. With halides being involved in the various structural arrangements, namely, pure corner-sharing MX (M is metal and X is halide) octahedra, for perovskite networks, or alternatively a combination of corner-, edge-, and/or face-sharing for related perovskitoids, they represent the ideal probe for characterizing the way octahedra are linked together. Well known for their inherently large quadrupolar constants, which is detrimental to the resolution of nuclear magnetic resonance spectroscopy, most abundant halide isotopes (Cl, Br, I) are in turn attractive for magnetic field-free nuclear quadrupolar resonance (NQR) spectroscopy.
View Article and Find Full Text PDFDalton Trans
December 2024
Department of Chemical Engineering, Indian Institute of Technology Madras, Adyar, Chennai, Tamil Nadu 600036, India.
Tuning the selectivity and improving the activity of photocatalysts are among the main bottlenecks for the conversion of CO to value-added chemicals. Recently, lead-free halide perovskites have been extensively investigated as photocatalysts for the photoreduction of CO. Herein, we report a composite photocatalyst using CsBiCl and Ir/IrO for the photoreduction of CO.
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